Evidence map›Paper›PMID 36638211›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

prM-reactive antibodies reveal a role for partially mature virions in dengue virus pathogenesis.

Kimberly A Dowd, Devika Sirohi, Scott D Speer, Laura A VanBlargan, Rita E Chen, Swati Mukherjee, Bradley M Whitener, Jennifer Govero, Maya Aleshnick, Bridget Larman and 10 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
5.8field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Application of Orthoflavivirus Pseudovirus Technology in Antiviral Research.International journal of molecular sciences · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. pr-independent biogenesis of infectious mature Zika virus particles.bioRxiv : the preprint server for biology · 2024
    Article
  13. Review
  14. Article
  15. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 1 country.

Kimberly A DowdViral Pathogenesis Section, Laboratory of Viral Diseases, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0003-3641-6852
Devika SirohiDepartment of Biological Sciences, Purdue University, West Lafayette, IN 47907.
Scott D SpeerViral Pathogenesis Section, Laboratory of Viral Diseases, National Institutes of Health, Bethesda, MD 20892.
Laura A VanBlarganDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Rita E ChenDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Swati MukherjeeViral Pathogenesis Section, Laboratory of Viral Diseases, National Institutes of Health, Bethesda, MD 20892.
Bradley M WhitenerDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0001-6652-0701
Jennifer GoveroDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Maya AleshnickViral Pathogenesis Section, Laboratory of Viral Diseases, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0001-5471-4242
Bridget LarmanViral Pathogenesis Section, Laboratory of Viral Diseases, National Institutes of Health, Bethesda, MD 20892.
Soila Sukupolvi-PettyDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110.
Madhumati SevvanaDepartment of Biological Sciences, Purdue University, West Lafayette, IN 47907.
Andrew S MillerDepartment of Biological Sciences, Purdue University, West Lafayette, IN 47907.
Thomas KloseDepartment of Biological Sciences, Purdue University, West Lafayette, IN 47907.ORCID 0000-0002-2150-9792
Aihua ZhengDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461.ORCID 0000-0002-2184-227X
Scott KoenigMacroGenics, Inc., Rockville, MD 20850.
Margaret KielianDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Richard J KuhnDepartment of Biological Sciences, Purdue University, West Lafayette, IN 47907.ORCID 0000-0003-4148-1026
Michael S DiamondDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110.ORCID 0000-0002-8791-3165
Theodore C PiersonViral Pathogenesis Section, Laboratory of Viral Diseases, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-3795-4348
National Institutes of Health · USWashington University in St. Louis · USPurdue University West Lafayette · USAlbert Einstein College of Medicine · USMacroGenics (United States) · US

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
The humoral response to Zika virus infection and vaccinationZIAAI001209 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI PIERSON, THEODORE · 2016 to 2025
$22.0M
Antibody-based Protection against FlavivirsesR01AI073755 · NIAID · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, FREMONT, DAVED H. · 2007 to 2022
$11.4M
Molecular Analysis of Alphavirus Membrane Fusion ProteinR01AI075647 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KIELIAN, MARGARET · 2007 to 2023
$9.0M
STRUCTURE OF A SMALL SPHERICAL VIRUSR01AI011219 · NIAID · PURDUE UNIVERSITY WEST LAFAYETTE · PI KUHN, RICHARD J. · 1985 to 2020
$2.4M
NIAID NIH HHS HHSN272201400018CNIAID NIH HHS R01 AI011219NIAID NIH HHS R01 AI073755NIAID NIH HHS R01 AI075647NIGMS NIH HHS T32 GM007200
6 · The paper itself

Abstract

Cleavage of the flavivirus premembrane (prM) structural protein during maturation can be inefficient. The contribution of partially mature flavivirus virions that retain uncleaved prM to pathogenesis during primary infection is unknown. To investigate this question, we characterized the functional properties of newly-generated dengue virus (DENV) prM-reactive monoclonal antibodies (mAbs) in vitro and using a mouse model of DENV disease. Anti-prM mAbs neutralized DENV infection in a virion maturation state-dependent manner. Alanine scanning mutagenesis and cryoelectron microscopy of anti-prM mAbs in complex with immature DENV defined two modes of attachment to a single antigenic site. In vivo, passive transfer of intact anti-prM mAbs resulted in an antibody-dependent enhancement of disease. However, protection against DENV-induced lethality was observed when the transferred mAbs were genetically modified to inhibit their ability to interact with Fcγ receptors. These data establish that in addition to mature forms of the virus, partially mature infectious prM

Indexed as

Antibodies, MonoclonalAntibodies, ViralDengueDengue VirusAnimalsCryoelectron MicroscopyMiceViral Envelope ProteinsVirionAntibodies, MonoclonalAntibodies, ViralViral Envelope Proteinsantibody-dependent enhancementdengue virusprM antibodyvirion maturation

Identifiers

PMID36638211
PMCPMC9933121
OpenAlexW4316015789

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.